EP0459619B1 - Copolymère de polyarylène-thioéthercétone et son procédé de préparation - Google Patents

Copolymère de polyarylène-thioéthercétone et son procédé de préparation Download PDF

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Publication number
EP0459619B1
EP0459619B1 EP91303614A EP91303614A EP0459619B1 EP 0459619 B1 EP0459619 B1 EP 0459619B1 EP 91303614 A EP91303614 A EP 91303614A EP 91303614 A EP91303614 A EP 91303614A EP 0459619 B1 EP0459619 B1 EP 0459619B1
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copolymer
charged
poly
mol
amount
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EP0459619A2 (fr
EP0459619A3 (en
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Yoshikatsu Satake
Yoshiyuki Inaguma
Yasuhiro Suzuki
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Kureha Corp
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Kureha Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/02—Polythioethers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/02—Polythioethers
    • C08G75/0204—Polyarylenethioethers
    • C08G75/0236—Polyarylenethioethers containing atoms other than carbon or sulfur in a linkage between arylene groups
    • C08G75/024—Polyarylenethioethers containing atoms other than carbon or sulfur in a linkage between arylene groups containing carbonyl groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/02—Polythioethers
    • C08G75/0204—Polyarylenethioethers
    • C08G75/0245—Block or graft polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds

Definitions

  • This invention relates to crystalline poly(arylene thioether-ketone) copolymers uniform in composition and excellent in heat resistance, melt stability, processability and handling properties, and more specifically to novel copolymers containing at least one poly(arylene thioether-ketone) segment [hereinafter abbreviated as "PTK segment (A)” or merely “segment (A)”] having predominant recurring units of the formula and at least one poly(arylene thioether) segment [hereinafter abbreviated as "PATE segment (B)” or merely “segment (B)”] having predominant recurring units of the formula and also to a process for the production thereof.
  • PTK segment (A) or merely “segment (A)”
  • PATE segment (B) poly(arylene thioether) segment
  • This invention is also concerned with a process for economically producing crystalline aromatic ketone copolymers by using inexpensive comonomers and polymerization solvent.
  • poly(arylene thioether-ketone) type polymers there have been proposed polymers having predominant recurring units of the following structural formula [III], [IV], [V] or [VI]:
  • the poly(arylene thioether-ketones) (hereinafter abbreviated as "PTKs") having the predominant recurring units of the structural formula [III] have excellent heat resistance, but involve a problem that they have poor heat stability upon melting (hereinafter called "melt stability”) (Japanese Patent Laid-Open Nos. 58435/1985 and 124/1989).
  • the polymers having the predominant recurring units of the structural formulae [IV] and [V], respectively, are not suitable for industrial production because they must use particular polymerization solvents and monomers (Japanese Patent Laid-Open Nos. 20017/1986, 197634/1986 and 27434/1987).
  • the poly(arylene thioether ketone ketones) (hereinafter abbreviated as "PTKKs") having the predominant recurring units of the structural formula [VI] have a melting point as extremely high as about 410°C. Their melt processing temperature are high accordingly, so that they tend to loss their crystallinity or to undergo cross-linking and/or carbonization, resulting in a rapid increase in melt viscosity, upon their melt processing.
  • PTKs and PTKKs contain ketone groups in their recurring units, they are poor in solvent resistance and moisture absorption resistance, so that their application fields as heat-resistant resins are unavoidably limited. PTKs and PTKKs are generally obtained as fine powders. This has led to an additional problem upon their production such that they show poor handling properties in their collection step after polymerization, especially in filtration, washing, drying and transportation. Still further problems have also arisen such as poor metering property upon melt processing and occurrence of blocking in hoppers or the like.
  • poly(p-phenylene thioether) as a poly(arylene thioether) (hereinafter abbreviated as "PATE") is used as high-performance engineering plastics having excellent heat resistance and solvent resistance.
  • PATE poly(p-phenylene thioether) as a poly(arylene thioether)
  • This polymer is obtained by reacting dichlorobenzene, which is very cheap and industrially available, with sodium sulfide (U.S. Patent Specification No. 3,919,177).
  • its crystalline melting point is about 285°C and its glass transition point (Tg) is also as low as about 85°C. There is thus a demand for development of polymers having a higher melting point and a higher Tg.
  • An object of this invention is to provide polymers with improved processability, handling properties and solvent resistance while retaining the excellent properties, such as heat resistance and crystallinity, of the aforementioned melt-stable PTKs as much as possible.
  • Another object of this invention is to provide a process for economically producing aromatic ketone copolymers having such properties.
  • the present inventors first of all attempted to lower the melting point, i.e., processing temperature of the PTK by random copolymerization of its monomer with monomers of a kind different from the first-mentioned monomer. Namely, 4,4′-dihalobenzophenone was used as a comonomer and copolymerized with dihalobenzene.
  • the resultant random copolymers tended to have lower crystallinity and heat resistance and poorer melt stability as the proportions of the dihalobenzenes increased.
  • 4,4′-dihalo-benzophenones have been activated by the ketone group and have far higher reactivity compared with dihalobenzenes. They hence have extremely poor copolymerizability with dihalobenzenes.
  • the present inventors then attempted to produce a PTK-PATE copolymer in which a PATE having recurring units of the formula is incorporated as segments in the chain of a PTK.
  • a poly(arylene thioether-ketone) copolymer having excellent processability and high crystallinity can be obtained by using as an oligomer a PATE, which has a particular number-average polymerization degree and contains at least one terminal thiolate group and/or thiol group as a reactive terminal group, and reacting the PATE oligomer with a 4,4′-dihalo-benzophenone under specific conditions in an organic amide solvent.
  • the present invention has been brought to completion on the basis of these findings.
  • a poly(arylene thioether-ketone) copolymer comprising (A) at least one poly(arylene thioether-ketone) segment having predominant recurring units of the formula wherein the -CO- and -S- are in the para position to each other and (B) at least one poly(arylene thioether) segment having predominant recurring units of the formula and having the following properties (a)-(c):
  • a process for the production of a poly(arylene thioether-ketone) copolymer comprising (A) at least one poly(arylene thioether-ketone) segment and (B) at least one poly(arylene thioether) segment, which comprises at least the following two steps:
  • a process for the production of a poly(arylene thioether-ketone) copolymer comprising (A) at least one poly(arylene thioether-ketone) segment and (B) at least one poly(arylene thioether) segment, which comprises at least the following three steps:
  • the poly(arylene thioether-ketone) copolymers according to the present invention are copolymers comprising (A) at least one PTK segment having predominant recurring units of the formula wherein the -CO- and -S- are in the para position to each other and (B) at least one PATE segment having predominant recurring units of the formula
  • the PTK segment (A) and the PATE segment (B) contain respectively the above-described recurring units in proportions of at least 50 wt.%, preferably at least 70 wt.%, particularly preferably at least 80 wt.%.
  • the recurring unit of the segment (B) is preferred because it can afford copolymers excellent especially from the viewpoint of crystallinity, melt stability, heat resistance, mechanical properties, solvent resistance, moisture absorption resistance and the like.
  • the copolymer of the present invention can have a desired structure containing both segments in an alternate order, such as (A) ⁇ (B)-(A) ⁇ m (B)-(A), m being 0 or an integer of 1 or greater or (A) ⁇ (B)-(A) ⁇ n (B), n being 0 or an integer of 1 or greater.
  • the weight ratio of the total amount of segments (B) to the total amount of segments (A) be within a range of 0.05-5, preferably 0.1-4, more preferably 0.15-3.
  • the segment (A) serves to impart high degree of heat resistance and crystallinity to the copolymer.
  • the segment (B) contributes to the reduction of the processing temperature and the granulation while maintaining the high crystallinity. Therefore, copolymers in each of which the weight ratio of the total amount of segments (B) to the total amount of segments (A) is at least 0.05 but lower than 1, preferably at least 0.1 but lower than 1 feature particularly good heat resistance and high crystallinity. Ratios in a range of 1-5, preferably 1-4 give copolymers excellent especially in processability while retaining excellent crystallinity.
  • any weight ratios of the total amount of segments (B) to the total amount of segments (A) lower than 0.05 are too low to achieve any sufficient reduction in processing temperature or the formation into granules.
  • any ratios higher than 5 lead to a substantial reduction in heat resistance and disturb the balancing between heat resistance and processability. Ratios outside the above range are therefore not preferred.
  • segment (B) it is essential for the segment (B) to have a number-average polymerization degree higher than 1 but lower than 10, preferably, in a range of 2-9, more preferably, in a range of 3-8.
  • the length of each segment in the copolymer according to the present invention is shortened, the melting point becomes sharp, and the uniformity in composition becomes high, so that preferred processability and physical properties can easily be achieved.
  • the resulting copolymer becomes similar to a block copolymer, so that it has physical properties characteristic of both PATE and PTK, for example, melting points corresponding to those thereof and requires a temperature higher than that of the copolymer according to the present invention upon its forming or molding. Therefore, its melt processing temperature becomes higher, so that melt processing facilities for high-temperature processing are required. Further, a stringent temperature control is required to perform melt processing without deterioration by heat. Furthermore, since each segment is long, the composition distribution of the copolymer becomes wider correspondingly. Polymerization degrees outside the above range are therefore not preferred.
  • the number-average polymerization degree of the PATE segment in this invention is determined by gel permeation chromatography (GPC) at a stage of the PATE oligomer. Measuring conditions are as follows: Column: SHODEX AT80M/S, two columns in series Solvent: ⁇ -chloronaphthalene Flow rate: 0.7 ml/min Temperature: 220°C Sample concentration: 0.05 wt.% Charged amount: 200 »l Detector: flame ionization detector (FID) Calibration of molecular weight: standard poly(styrene) and Data processing: SIC 7000B (manufactured by System Instrument Co.)
  • the segment (A) and segment (B) can contain one or more recurring units other than their predominant recurring units of the formulae and to an extent that the objects of the present invention are not impaired.
  • these other recurring units can be introduced into the copolymers by using the corresponding various dihalogenated aromatic compounds as comonomers.
  • the melting point of PTK homopolymer as polymerized is about 360°C.
  • the extent of a reduction in the melting point due to copolymerization with another monomer of a different kind, ⁇ Tm [360°C - Tm (melting point of copolymer)] is generally proportional to the extent of a reduction in the melt processing temperature. Accordingly, ⁇ Tm can be used as an index indicative of processing temperature reducing effect, namely, processability improving effect.
  • ⁇ Tm may preferably be 10-80°C, more preferably 20-70°C, most preferably 30-65°C. If ⁇ Tm is lower than 10°C, there is a potential problem that the processability improving effect may not be sufficient. If ⁇ Tm is higher than 80°C on the other hand, there is another potential problem that the copolymer may lose the characteristics as a heat-resistant resin. ⁇ Tm outside the above range is therefore not preferred.
  • copolymers according to this invention have not only excellent processability but also high crystallinity. Crystallinity imparts high heat resistance to a copolymer. To have a copolymer equipped with high heat resistance, it is essential that the copolymer has sufficient crystallinity.
  • melt crystallization enthalpy, ⁇ Hmc is proportional to the degree of crystallization when a molten polymer undergoes crystallization.
  • melt crystallization temperature, Tmc serves as an index of the readiness of crystallization. Therefore, the melt crystallization enthalpy, ⁇ Hmc (400°C) and melt crystallization temperature, Tmc (400°C) of a copolymer according to this invention as measured when cooled at a rate of 10°C/min immediately after being heated to 400°C in an inert gas atmosphere by means of a differential scanning calorimeter (hereinafter abbreviated as "DSC") can be used as indices of the crystallinity of the copolymer.
  • DSC differential scanning calorimeter
  • melt crystallization enthalpy, ⁇ Hmc (400°C/10 min) and melt crystallization temperature, Tmc (400°C/10 min) measurable upon determination of the residual crystallinity can be used as an index of not only melt stability but also crystallinity.
  • the copolymers according to this invention may preferably have ⁇ Hmc (400°C) of at least 15 J/g, more preferably at least 20 J/g, most preferably at least 25 J/g.
  • Tmc (400°C) may desirably be at least 180°C, with at least 190°C being more preferred.
  • Copolymers having ⁇ Hmc (400°C) smaller than 15 J/g or Tmc (400°C) lower than 180°C may have insufficient heat resistance as heat-resistant polymers and are hence not preferred.
  • copolymers according to this invention have melt stability sufficient to permit the application of conventional melt processing techniques.
  • Polymers of poor melt stability tend to lose their crystallinity or to undergo crosslinking or carbonization, resulting in a rapid increase in melt viscosity, upon melt processing. It is hence possible to obtain an index of the melt processability of a polymer by investigating the residual crystallinity of the polymer after holding it at an elevated temperature of its melt processing temperature or higher for a predetermined period of time.
  • the residual crystallinity can be evaluated quantitatively by measuring the melt crystallization enthalpy of the polymer by a DSC.
  • indices of the melt stability of a copolymer its residual melt crystallization enthalpy, ⁇ Hmc (400°C/10 min) and melt crystallization temperature, Tmc (400°C/10 min), which are determined at a cooling rate of 10°C/min after the copolymer is held at 50°C for 5 minutes in an inert gas atmosphere, heated to 400°C at a rate of 75°C/min and then held for 10 minutes at 400°C which is higher than the melt processing temperature of the copolymer.
  • ⁇ Hmc 400°C/10 min
  • Tmc melt crystallization temperature
  • the copolymers of this invention are polymers having the physical properties that their residual melt crystallization enthalpies, ⁇ Hmc (400°C/10 min) are at least 10 J/g, more preferably at least 15 J/g, most preferably at least 20 J/g and their melt crystallization temperatures, Tmc (400°C/10 min) are at least 170°C, more preferably at least 180°C, most preferably at least 190°C.
  • a polymer whose ⁇ Hmc (400°C/10 min) is smaller than 10 J/g or whose Tmc (400°C/10 min) is lower than 170°C, tends to lose its crystallinity or to induce a melt viscosity increase upon melt processing, so that difficulties are encountered upon application of conventional melt processing techniques.
  • the ratio of melt crystallization enthalpy to residual melt crystallization enthalpy namely, ⁇ Hmc (400°C)/ ⁇ Hmc (400°C/10 min) can also be used as an index of melt stability. Deterioration by heat becomes smaller as this ratio decreases. Therefore, it is preferably that ⁇ Hmc (400°C/10 min) is at least 10 J/g and the above ratio is 5 or smaller, more preferably 3 or smaller.
  • the melt viscosity, ⁇ * of each copolymer is used as an index of its molecular weight.
  • a polymer sample is filled in a Capirograph manufactured by Toyo Seiki Seisaku-Sho, Ltd. and equipped with a nozzle having an inner diameter of 1 mm and an L/D ratio of 10/1 and is preheated at 350°C for 5 minutes. Its melt viscosity, ⁇ * is measured at a shear rate of 1,200/sec.
  • the copolymers of the present invention have a melt viscosity, ⁇ * of 2-100,000 poises (0.2-104 Pa.s), preferably 5-50,000 poises (0.5-5,000 Pa.s), more preferably 10-30,000 poises (1-3000 Pa.s).
  • Those having a melt viscosity, ⁇ * lower than 2 poises have an unduly low molecular weight, so that their flowability is too high to conduct conventional melt processing. Even if melt-formed or melt-molded products are obtained, their physical properties are considerably inferior. Such low melt viscosities are therefore not preferred.
  • those having a melt viscosity, ⁇ * higher than 100,000 poises have an unduly high molecular weight, so that their flowability is too low to conduct conventional melt processing. Such high melt viscosities are therefore not preferred either.
  • an alkali metal sulfide and a dihalogenated aromatic compound are employed as principal raw materials for the polymer, amd as reaction polymerization media are employed an organic amide solvent and water including water of hydration.
  • sodium sulfide is industrially preferred for its low price.
  • An alkali metal sulfide which may be formed in situ in the reaction system can also be used.
  • the dihalogenated aromatic compound employed in the present invention for the formation of the PTK segment (A), including a PTK oligomer, consists principally of one or more dihalobenzophenones, i.e., 4,4′-dichlorobenzophenone and/or 4,4′-dibromobenzophenone.
  • the dihalogenated aromatic compound used in the present invention for the formation of the PATE segment (B), including a PATE oligomer, consists principally of a dihalobenzene such as p-dichlorobenzene or m-dichlorobenzene.
  • dihalobenzophones other than 4,4′-isomers dihaloalkylbenzenes, dihalobiphenyls, dihalodiphenyl sulfones, dihalonaphthalenes, bis(halogenated phenyl)methanes, dihalopyridines, dihalothiophenes and dihalobenzonitriles, and mixtures thereof.
  • substituent halogen atoms chlorine or bromine atoms may be used preferably from the economical viewpoint.
  • a small amount of a fluorine compound for example, difluorobenzophenone or the like may also be used in combination.
  • aprotic polar organic solvents having excellent heat stability and alkali resistance can be used.
  • organic amide solvents including carbamic amides, and sulfone solvents are particularly preferred.
  • organic amide solvents and sulfone solvents may be mentioned N-methylpyrrolidone, N-ethylpyrrolidone, N,N′-ethylenedipyrrolidone, pyrrolidones, hexamethylphosphoric triamide, tetramethylurea, dimethylimidazolidinone, dimethylacetamide, ⁇ -caprolactam, N-ethylcaprolactam, sulfolane, diphenyl sulfone, etc. They may also be used as a mixed solvent.
  • N-methylpyrrolidone or its mixed solvent is particularly preferred from the viewpoint of the readiness in obtaining a melt-stable copolymer, thermal and chemical stability, economy, etc.
  • the PATE oligomer employed as a raw material for the copolymer of this invention can be prepared by having an alkali metal sulfide and a dihalogenated aromatic compound, which consists principally of a dihalobenzene, undergo a reaction in the presence of water in an organic amide solvent under the following conditions (a)-(c):
  • the PATE oligomer formed has at least one terminal thiolate group.
  • the oligomer having at least one terminal thiolate group means an oligomer having a thiolate group on its each terminal or one terminal, or a mixture thereof.
  • the PATE oligomer may contain some crosslinked structure and/or branched structure introduced typically by allowing a trihalobenzene or higher polyhalobenzene to present in a small amount in the polymerization reaction system. Incidentally, among the recurring units of the formula the recurring unit of the formula is preferred.
  • the PTK oligomer employed as a raw material for the copolymer of this invention can be prepared in the following manner.
  • the PTK oligomer can be prepared by having an alkali metal sulfide and a dihalogenated aromatic compound, which consists principally of 4,4′-dichlorobenzophenone and/or 4,4′-dibromobenzophenone, undergo a reaction in the presence of water in an organic amide solvent under the following conditions (a)-(b):
  • the PTK oligomer has at least one terminal halogen atom.
  • the PTK oligomer may contain some crosslinked structure and/or branched structure introduced typically by allowing a trihalobenzophenone or higher polyhalobenzophenone to present in a small amount in the polymerization reaction system.
  • the reduced viscosity of the PTK oligomer is 0.2 dl/g or lower, preferably 0.1 dl/g or lower, more preferably 0.05 dl/g or lower as determined by viscosity measurement at 30°C and a polymer concentration of 1.0 g/dl in 98% concentrated sulfuric acid.
  • the ratio of the amount of the charged dihalogenated aromatic compound to the amount of the charged alkali metal sulfide upon synthesis of the PTK oligomer may preferably be at least 1.15 (mol/mol), more preferably at least 1.2 (mol/mol), most preferably at least 1.3 (mol/mol).
  • it is desirable to charge the organic amide solvent in general, in an amount of 0.6-100 kg, more preferably 0.7-50 kg per mole of the amount of the charged alkali metal sulfide, depending upon the composition of the charged dihalogenated aromatic compound.
  • each copolymer may be described the process (Production Process No. 1) in which a PATE oligomer is prepared in advance and at least one PTK segment is formed in the presence of the PATE oligomer.
  • This process is substantially a two-step process.
  • the reaction mixture containing the oligomer obtained in the first step may be mixed with a dihalogenated aromatic compound consisting principally of at least one dihalobenzophenone selected from 4,4′-dichlorobenzophenone and 4,4′-dibromobenzophenone, and the resultant mixture may be heated without further addition of any alkali metal sulfide, organic amide solvent or water, thereby obtaining a copolymer. It goes without saying that the alkali metal sulfide, organic amide solvent or water may be added further in the second step.
  • the water content in the reaction system may desirably be within a range of 0.1-15 moles, preferably 2.5-15 moles, more preferably 3.5-14 moles per kg of the amount of the charged organic amide solvent.
  • Water contents lower than 0.1 mole can hardly provide a copolymer having high melt stability and moreover tend to induce decomposition in the polymerization reaction.
  • water contents higher than 15 moles result in a reduction in the reaction rates, so that the reaction requires an unduly long period of time. Such high water contents are hence not preferred in industry.
  • the water content may be reduced by distillation or the like or may be increased by adding water prior to the initiation of a polymerization reaction.
  • the ratio of the total amount of the dihalogenated aromatic compound to the total amount of the alkali metal sulfide, both charged upon synthesis of the copolymer may desirably be in a range of 0.95-1.2 (mol/mol), more preferably 0.97-1.10 (mol/mol), most preferably 0.98-1.05 (mol/mol).
  • the term "the total amount of the charged alkali metal sulfide” means the sum of the amount of the alkali metal sulfide charged upon synthesis of the PTK oligomer and/or the PATE oligomer and the amount of the alkali metal sulfide charged upon synthesis of the copolymer.
  • Ratios smaller than 0.95 can hardly provide a copolymer having excellent melt stability and tend to induce decomposition during the reaction.
  • ratios greater than 1.2 can only provide a copolymer having a low molecular weight.
  • it is desirable to charge the organic amide solvent in general, in an amount of 0.3-5 kg, more preferably 0.4-3 kg per mole of the amount of the charged alkali metal sulfide, depending upon the composition of the charged dihalogenated aromatic compound.
  • the term "the amount of the charged alkali metal sulfide" as used herein means the remaining amount which is obtained by subtracting the loss from the amount actually charged.
  • the segment (A) serves to impart high degree of heat resistance and crystallinity to the copolymer.
  • the segment (B) contributes to the reduction of the processing temperature and the granulation while maintaining the high crystallinity. Accordingly, the ratio of the charged amount of the dihalogenated aromatic compound consisting principally of the dihalobenzene in the first step to the charged amount of the dihalogenated aromatic compound consisting principally of the dihalobenzophenone in the second step is controlled within a range of 0.1-10 (mol/mol), preferably 0.2-7.5 (mol/mol), more preferably 0.3-6.0 (mol/mol).
  • copolymers in each of which this ratio is within a range of 0.1-1.9, preferably 0.2-1.9 feature particularly good heat resistance and high crystallinity.
  • Ratios in a range of 2-10, preferably 2-7.5 give copolymers excellent especially in processability while retaining excellent crystallinity.
  • any ratios lower than 0.1 are too low to achieve any sufficient reduction in processing temperature or the formation into granules.
  • any ratios higher than 10 lead to a substantial reduction in heat resistance and disturb the balancing between heat resistance and processability. Ratios outside the above range are therefore not preferred.
  • the amount of the charged dihalogenated aromatic compound should be interpreted not to include the amount of the halogen-substituted aromatic compound added in the final stage of the reaction for effecting a stabilizing treatment to be described subsequently.
  • reaction temperatures lower than 150°C require an unduly long time to obtain the copolymer and are therefore economically disadvantageous.
  • reaction temperatures higher than 300°C can hardly obtain the copolymer in a form excellent in melt stability and moreover involve a potential problem of decomposition during the reaction.
  • the polymerization time required for obtaining a PTK oligomer or copolymer of a desired molecular weight becomes shorter as the polymerization temperature increases but becomes longer as the polymerization temperature decreases. Accordingly, it is generally advantageous to conduct the polymerization at a temperature of 210°C or higher from the viewpoint of productivity. It is however not preferred to conduct the reaction at a temperature of 210°C or higher for 10 hours or longer, because a PTK oligomer or copolymer having excellent melt stability can hardly be obtained under such conditions.
  • a reactor including equipment employed for provisional procedures of the polymerization reaction, for example, those required for dehydration and the like
  • a reactor which is made of a corrosion-resistant material at least at portions with which the reaction mixture is brought into direct contact.
  • the corrosion-resistant material is supposed to be inert so that it does not react with the reaction mixture.
  • the corrosion-resistant material include titanium materials such as titanium and titanium-containing alloys and nickel-containing corrosion-resistant materials. Of these, it is particularly preferred to use a reactor lined with a titanium material.
  • the copolymer can be obtained in a form improved further in melt stability by adding a certain kind of halogen-containing compound to the reaction system and causing it to undergo a reaction in a final stage of the reaction.
  • halogen-containing compounds may be mentioned C1-C3 alkyl halides and halogen-substituted aromatic compounds. It is particularly preferable to use at least one halogen-substituted aromatic compound which contains at least one group having electron-withdrawing property at least equal to -CO- group.
  • a halogen-substituted aromatic compound may be mentioned bis(chlorobenzoyl)benzenes, dihalobenzophenones, dihalodiphenylsulfones, monohalobenzophenones and the like, and mixtures thereof.
  • Another principal feature of the process of this invention for the production of the copolymer resides in that the copolymer excellent in melt stability can be obtained as granules by suitably choosing the aforementioned reaction conditions for the copolymer further. Reaction conditions for obtaining at least 50 wt.% of the resulting copolymer as granules collectible by means of a sieve having an opening size of 75 »m (200 mesh) will next be described in further detail.
  • the weight proportion of segment or segments (B) in the copolymer is an important parameter since each segment (B) contributes to the granulation.
  • reaction temperature it is desirable to raise the reaction temperature to a high temperature of at least 240-290°C, more preferably 250-290°C in the course of the reaction or in a final stage of the reaction. Reaction temperatures lower than 240°C make it difficult to obtain the copolymer as granules. On the contrary, it is difficult to obtain the copolymer in a form excellent in melt stability if the reaction temperature is higher than 290°C.
  • the time required for obtaining the copolymer as desired granules becomes shorter as the reaction temperature increases. Conversely, it becomes longer as the reaction temperature decreases. Therefore, it is generally advantageous from the viewpoint of productivity to conduct the reaction at a high temperature of 250°C or higher. It however becomes difficult to obtain the copolymer in a form excellent in melt stability if the reaction at high temperatures of 250°C and higher is continued for 7 hours or longer.
  • the following method can be followed. Namely, after completion of the reaction including the treatment in the final stage if applied, the reaction mixture is subjected to flushing and/or distillation, whereby the solvent is removed either partly or wholly to concentrate the reaction mixture. If necessary, the concentrate may be heated to remove any remaining solvent. The resulting solids or concentrate is washed with water and/or an organic solvent to eliminate soluble components such as salts formed in the reaction. The residue is again dried under heat to collect the polymer.
  • At least 50 wt.% of the resulting copolymer can be obtained as granules which can be captured on a screen having an opening size of 75 »m (200 mesh), more preferably 106 »m (140 mesh), most preferably 150 »m (100 mesh).
  • the copolymer can be easily collected as granules by a screen or the like from the reaction mixture after completion of the reaction.
  • the granular polymer thus collected is washed with water and/or an organic solvent and then dried under heat to obtain it in a dry form. Since the copolymer is in a granular form and has excellent handling property, it permits easy separation, water washing, transportation, metering and the like.
  • the copolymers according to the present invention are crystalline and permit the application of conventional melt processing techniques. They can be formed or molded into various heat-resistant products and can then be used in various fields.
  • extrusion products may include sheets, plates, pipes, tubes, covered conductors, etc.
  • Injection-molded products may be used as electronic and electric parts, car parts, etc.
  • unstretched films may be employed as base films for magnetic recording, capacitor films, printed circuit boards, insulating films, prepreg sheets, and so on.
  • the present invention can provide crystalline poly(arylene thioether-ketone) copolymers uniform in composition and excellent in heat resistance, melt stability, processability and handling properties.
  • the invention can also economically provide such poly(arylene thioether-ketone) copolymers.
  • the invention can also provide various formed or molded products of such poly(arylene thioether-ketone) copolymers.
  • a titanium-lined reactor was charged with 3200 g of hydrated sodium sulfide (water content: 53.8 wt.%) and 6000 g of N-methylpyrrolidone (hereinafter abbreviated as "NMP"). While gradually heating the contents to 203°C in a nitrogen gas atmosphere, 2376 g of an NMP solution, which contained 1309 g of water, and 12.98 g of hydrogen sulfide were distilled out. Thereafter, 103 g of water was added.
  • NMP N-methylpyrrolidone
  • a portion of Reaction Slurry S1 was sampled out, and the amount of the remaining monomer and the number-average polymerization degree were determined.
  • the amount of PDCB (remaining monomer) in the reaction slurry as determined by gas chromatography was lower than 0.1 wt.% of the charged amount.
  • the number-average polymerization degree of Oligomer P1 was 5.
  • the number-average polymerization degree was determined by preparing a sample in the following manner and subjecting it to high-temperature GPC. Immediately after completion of the polymerization of the oligomer, a portion of the reaction slurry was sampled out and then poured into water, and the water was adjusted to a pH of 3.0 with hydrochloric acid to have the oligomer precipitated. The oligomer was collected by filtration, thoroughly washed in distilled water and then dried at room temperature under reduced pressure in a vacuum drier, thereby obtaining an oligomer sample.
  • the thus-obtained oligomer sample was added to ⁇ -chloronaphthalene to a concentration of 0.05 wt.% and dissolved therein under heat, thereby preparing a sample solution for GPC.
  • the measuring conditions for high-temperature GPC are as described above.
  • a titanium-lined reactor was charged with 8.0 g of hydrated sodium sulfide (water content: 53.8 wt.%), 63.4 g of 4,4′-dichlorobenzophenone (hereinafter abbreviated as "DCBP"), 501 g of Reaction Slurry S1 thus obtained, 278 g of NMP and 89.7 g of water. After the reactor being purged with nitrogen, the contents were heated to 265°C at which they were polymerized for 0.5 hour. To conduct the stabilizing treatment in the final stage of polymerization, the reaction mixture was cooled to 240°C, in which a mixture of 7.5 g of DCBP and 70 g of NMP was put under pressure to react them at 240°C for 0.5 hour.
  • DCBP 4,4′-dichlorobenzophenone
  • the resulting reaction mixture in the form of a slurry was diluted with a substantially equiamount of NMP and the granular polymer thus obtained was collected by a screen having an opening size of 150 »m (100 mesh).
  • the polymer was washed three times with NMP and further three times with water, and then dried at 100°C for 24 hours under reduced pressure to obtain a copolymer (Copolymer C1).
  • the collection rate of Copolymer C1 was 88%.
  • Copolymer C1 was in the form of granules having an average particle size of about 600 »m.
  • IR infrared
  • a strong absorption peak attributed to ketone group was observed at 1640 cm ⁇ 1.
  • Wide angle X-ray diffraction which was conducted using "RAD-B System” manufactured by Rigaku Denki Kabushiki Kaisha showed a diffraction pattern apparently different from that corresponding to PATE homopolymer, PTK homopolymer or a blend thereof, or a block copolymer of PATE and PTK.
  • the content of sulfur in Copolymer C1 was determined by means of a sulfur analyzer ("EMIA-510" manufactured by Horiba Ltd.).
  • the weight fraction W b (wt.%) of the recurring units in the copolymer can be calculated in accordance with the following equation and was 51%.
  • W b (W - W1)/(W2 - W1) x 100 wherein W means the weight fraction of sulfur in the copolymer, W1 denotes the weight fraction of sulfur in PTK recurring unit, and W2 represents the weight fraction of sulfur in PATE recurring unit.
  • the melt viscosity of Copolymer C1 was 350 poises (35 Pa.s). Tmc and ⁇ Hmc are shown in Table 1. Incidentally, the copolymer as polymerized had a melting point (Tm) of 312°C.
  • the amount of PDCB (remaining monomer) in the reaction slurry as determined in the same manner as in Example 1 was 0.1 wt.% of the charged amount.
  • the number-average polymerization degree of the resultant oligomer (Oligomer P2) was 5.
  • a titanium-lined 1-l reactor was charged with 682.9 g of the thus-obtained Reaction Slurry S2 and 69.3 g of DCBP. After the reactor being purged with nitrogen, the contents were heated to 240°C at which they were polymerized for 3 hours.
  • the resulting reaction mixture in the form of a slurry was filtered by a filter paper (class: 5A) to collect solids.
  • the thus-collected solids were washed with acetone and water repeatedly and then dried at 100°C, thereby obtaining a copolymer (Copolymer C2).
  • the collection rate of Copolymer C2 was 96%.
  • Copolymer C2 The physical properties of Copolymer C2 are shown in Table 1.
  • the melt viscosity of Copolymer C2 was 60 poises (6 Pa.s).
  • Copolymer C2 was soluble in concentrated sulfuric acid, and its reduced viscosity was 0.28 dl/g as measured at 30°C and a polymer concentration of 0.4 g/dl.
  • a titanium-lined reactor was charged with 3.20 kg of hydrated sodium sulfide (water content: 53.8 wt.%) and 6.00 kg of NMP. While gradually heating the contents to 203°C in a nitrogen gas atmosphere, 2.326 kg of an NMP solution, which contained 1.282 kg of water, and 10.27 g of hydrogen sulfide were distilled out. Thereafter, 0.076 kg of water was added.
  • a portion of the reaction slurry was sampled out, and the amount of the remaining monomer and the number-average polymerization degree were determined in the same manner as in Example 1. As a result, the amount of the remaining monomer was lower than 0.1 wt.% of the charged amount, and the number-average polymerization degree of Oligomer P3 was 8.
  • Slurry KS1 reaction slurry
  • PTK oligomer K1 PTK oligomer
  • the oligomer was collected by filtration, thoroughly washed in distilled water and then dried at room temperature under reduced pressure in a vacuum drier, thereby obtaining an oligomer sample.
  • the thus-obtained oligomer sample was dissolved in 98% concentrated sulfuric acid to give a concentration of 1.0 g/dl so as to measure the reduced viscosity of the oligomer at 30°C.
  • the reduced viscosity was extremely low and the value was lower than 0.05 dl/g.
  • a titanium-lined reactor was charged with 448 g of Reaction Slurry S3 containing PATE Oligomer P3, 377 g of Reaction Slurry KS1 containing PTK Oligomer K1 and 64 g of water. After the reactor being purged with nitrogen, the contents were maintained at 265°C for 0.5 hour to react them. To conduct the stabilizing treatment in the final stage of polymerization, the reaction mixture was cooled to 240°C, in which a mixture of 7.5 g of DCBP and 70 g of NMP was put under pressure to react them at 240°C for 0.5 hour.
  • the resulting reaction mixture in the form of a slurry was diluted with a substantially equiamount of NMP and the granular polymer thus obtained was collected by a screen having an opening size of 150 »m (100 mesh).
  • the polymer was washed three times with NMP and further three times with water, and then dried at 100°C for 24 hours to obtain a copolymer (Copolymer C3) in the form of granules having an average particle size of 1200 »m.
  • the collection rate was 80%.
  • the melt viscosity of Copolymer C3 was 610 poises (61 Pa.s). Physical properties such as Tmc and ⁇ Hmc are shown collectively in Table 1. Incidentally, Tm of the copolymer as polymerized was 316°C.
  • the polymer was collected by filtration, and then washed twice with acetone and additionally twice with water. Acetone and water were removed to obtain the polymer in a wet form.
  • the wet polymer was dried at 80°C for 24 hours, thereby obtaining a polymer (Polymer R1) as an ivory powder.
  • the particle size of Polymer R1 thus obtained was measured by an image analyzer ("OMNICON", trade mark; manufactured by Shimadzu Corp.). The average particle size was 10.6 »m. Particles not greater than 6»m amounted to 60.5 wt.%. On the other hand, particles of 30 »m and greater accounted for 0.4 wt.% only.
  • the bulk density of Polymer R1 was 0.24 g/dl.
  • Tm of the polymer as polymerized was 362°C. Polymer R1 thus obtained was soluble in 98% concentrated sulfuric acid but was insoluble in ⁇ -chloronaphthalene even at 225°C.
  • a titanium-lined 1-l reactor was charged with 35 g of fine particulate PTK Polymer R1 obtained in Comparative Example 1 and 65 g of poly(p-phenylene thioether) ("FORTRON #W214", trade mark, product of Kureha Chemical Industry Co., Ltd.) and further with 500 g of NMP and 45 g of water. The contents were maintained at 260°C for 2 hours. After cooling, the resultant slurry was passed through a screen having an opening size of 75 »m (200 mesh) to collect a particulate polymer. From the filtrate, a fine powdery polymer was also collected using a filter paper (class: 5A). The polymers thus collected were separately washed and dried in a similar manner to Example 1, thereby obtaining 51 g of granular Polymer R2 and 37 g of fine powdery polymer.
  • the remaining monomer was founded to be PDCB. Its amount was equal to 33% of the amount charged.
  • the slurry as the reaction mixture was passed through a screen having an opening size of 75 »m (200 mesh). It was however unable to collect any granular polymer.
  • a titanium-lined 1-l reactor was charged with 106 g of the fine powdery PTK polymer obtained in Comparative Example 1 and also with 500 g of NMP and 45 g of water. The contents were maintained at 260°C for 2 hours. After cooling, the resultant slurry was passed through a screen having an opening size of 75 »m (200 mesh). It was however unable to collect any granular polymer.
  • a titanium-lined 1-l reactor was charged with 0.5 mole of DCBP, 0.5 mole of hydrated sodium sulfide (water content: 54.0 wt.%) and 500 g of NMP. After the reactor being purged with nitrogen, the resultant mixture was maintained at 260°C for 2 hours to react them. The reactor was cooled, and the reaction mixture in the form of a slurry was passed through a screen having an opening size of 75 »m (200 mesh). It was however unable to collect any granular polymers.
  • a charge pot equipped with a heater was mounted on the titanium-lined 20-l reactor with the reaction slurry containing the PTK prepolymer (temperature of slurry: 220°C).
  • the pot was charged with 9.12 kg of the reaction slurry containing the PATE prepolymer.
  • the PATE prepolymer-containing reaction slurry was heated to 220°C and then added to the PTK prepolymer-containing reaction slurry. Further, 1.146 kg of water was added, and the contents were then mixed. The contents were maintained at 260°C for 2 hours to react them. After the contents being allowed to cool down to 240°C, a final treatment of the reaction was conducted.
  • the final stabilizing treatment of the reaction was effected by adding 0.4356 mole of DCBP and 0.5 kg of NMP and then reacting the contents at 240°C for 0.2 hour.
  • Block Copolymer B1 The physical properties of Block Copolymer B1 are shown in Table 1.
  • Block Copolymer B1 With respect to Block Copolymer B1, a plurality of peaks corresponding to its melting points appear, and the peak width at half height is great. Regarding the copolymers according to this invention on the other hand, the peak corresponding to the melting point is single and sharp. This indicates that their uniformity in composition is excellent. Incidentally, the melt viscosity of Block Copolymer B1 was 650 poises (65 Pa.s).
  • Copolymer C1 Block Copolymer B1 synthesized in Comparative Example 7
  • PTK Homopolymer R1 synthesized in Comparative Example 1 and poly(p-phenylene thioether) ("FORTRON #W214", trade mark; product of Kureha Chemical Industry Co., Ltd.) were separately hot-pressed and then cooled to form amorphous sheets.
  • the respective amorphous sheets were placed in the solvents shown in Table 2 to investigate their dissolution behavior.
  • Copolymer C1 have solubility characteristics different from the PTK homopolymer and poly(p-phenylene thioether) which are homopolymers of the components of the copolymer, and the PATE-PTK block copolymer.
  • the sulfur content of the precipitate from the solution was determined.
  • Block Copolymer B1 the sulfur content of the precipitate was more than that of the original polymer before the dissolution by several percent. Namely, it is understood that Copolymer C1 according to this invention is uniform in composition distribution compared with Block Copolymer B1.
  • a titanium-lined reactor was charged with 488 g of the resulting Reaction Slurry S5, 63.4 g of DCBP, 278 g of NMP, 18.9 g of water and 16.4 g of hydrated sodium sulfide (water content: 53.98 wt.%). After the reactor being purged with nitrogen gas, the contents were heated to 265°C at which they were reacted for 0.5 hour. After the contents being allowed to cool down to 240°C, a final treatment of the reaction was conducted. The final stabilizing treatment of the reaction was effected by putting under pressure a mixture of 7.5 g of DCBP, 43 g of NMP and 4.3 g of water in the reaction mixture to react them at 240°C for 0.5 hour.
  • the reaction conditions upon synthesis of the copolymer were as follows:
  • Copolymer C5 The physical properties of Copolymer C5 were as follows: Melt viscosity: 70 poises (7 Pa.s) Transition temperature: Tg: 112°C (as to quench-pressed sheet) Tm: 315°C (as to polymer as polymerized) Tm: 302°C (as to quench-pressed sheet) Melt crystallization temperature: Tmc (400°C): 260°C Tmc (400°C/10 min): 220°C Melt crystallization enthalpy: ⁇ Hmc (400°C): 47 J/g Residual melt crystallization enthalpy: ⁇ Hmc (400°C/10 min): 31 J/g Incidentally, the weight ratio of the sum of PATE recurring units to the sum of PTK recurring units was 0.99.
  • reaction slurry (Slurry S6) containing a PPTE oligomer (Oligomer P6, number-average polymerization degree: 8) was obtained in a similar manner to Example 5.
  • a titanium-lined reactor was charged with 587.0 g of Reaction Slurry S6 and 296.1 g of Reaction Slurry KS6. After the reactor being purged with nitrogen, the contents were heated to 265°C at which they were reacted for 0.5 hour.
  • the reaction conditions upon synthesis of the copolymer were as follows:
  • Example 6 Collection was conducted in the same manner as in Example 1, thereby obtaining a copolymer (Copolymer C6).
  • the collection rate was 71% when recovered by means of a screen having an opening size of 150 »m.
  • Copolymer C6 The physical properties of Copolymer C6 were as follows: Melt viscosity: 90 poises (9 Pa.s) Transition temperature: Tg: 102°C (as to quench-pressed sheet) Tm: 297°C (as to polymer as polymerized) Tm: 294°C (as to quench-pressed sheet) Melt crystallization temperature: Tmc (400°C): 261°C Tmc (400°C/10 min): 214°C Melt crystallization enthalpy: ⁇ Hmc (400°C): 54 J/g Residual melt crystallization enthalpy: ⁇ Hmc (400°C/10 min): 42 J/g Incidentally, the weight ratio of the sum of PATE recurring units to the sum of PTK recurring units was 1.5.
  • the number-average polymerization degree of Oligomer P7 was 8.
  • a titanium-lined reactor was charged with 488.0 g of Reaction Slurry S7 and 376.8 g of Reaction Slurry KS7. After the reactor being purged with nitrogen, the contents were heated to 265°C at which they were reacted for 0.5 hour. After the contents being allowed to cool down to 240°C, a final treatment of the reaction was conducted. The final stabilizing treatment of the reaction was effected by putting under pressure a mixture of 7.5 g of DCBP, 42.8 g of NMP and 4.3 g of water in the reaction mixture to react them at 240°C for 0.5 hour.
  • the reaction conditions upon synthesis of the copolymer were as follows:
  • Example 7 Collection was conducted in the same manner as in Example 1, thereby obtaining a copolymer (Copolymer C7).
  • the collection rate was 73% when recovered by means of a screen having an opening size of 150 »m.
  • Copolymer C7 The physical properties of Copolymer C7 were as follows: Melt viscosity: 90 poises (9 Pa.s) Transition temperature: Tg: 110°C (as to quench-pressed sheet) Tm: 314°C (as to polymer as polymerized) Tm: 302°C (as to quench-pressed sheet) Melt crystallization temperature: Tmc (400°C): 266°C Tmc (400°C/10 min): 224°C Melt crystallization enthalpy: ⁇ Hmc (400°C): 52 J/g Residual melt crystallization enthalpy: ⁇ Hmc (400°C/10 min): 38 J/g Incidentally, the weight ratio of the sum of PATE recurring units to the sum of PTK recurring units was 0.99.
  • a portion of the reaction slurry thus obtained was treated in the same manner as in Example 3 to determine the reduced viscosity of the oligomer sample.
  • the reduced viscosity was extremely low and the value was lower than 0.05 dl/g.
  • a charge pot equipped with a heater was mounted on the titanium-lined reactor with the reaction slurry containing the PTK oligomer (temperature of slurry: 180°C). The pot was charged with 9039 g of the reaction slurry containing the PATE oligomer. The PATE oligomer-containing reaction slurry was heated to 180°C and then added to the PTK oligomer-containing reaction slurry. Further, 1242 g of water was added, and the contents were then mixed.
  • the contents were maintained at 265°C for 30 minutes to react them. After the contents being allowed to cool down to 240°C, a final treatment of the reaction was conducted. The final stabilizing treatment of the reaction was effected by adding 137 g of DCBP and 776 g of NMP and then reacting the contents at 240°C for 30 minutes.
  • the reaction conditions upon synthesis of the copolymer were as follows:
  • Copolymer C8 The physical properties of Copolymer C8 were as follows: Melt viscosity: 250 poises (25 Pa.s) Transition temperature: Tg: 112°C (as to quench-pressed sheet) Tm: 313°C (as to polymer as polymerized) Tm: 297°C (as to quench-pressed sheet) Melt crystallization temperature: Tmc (400°C): 265°C Tmc (400°C/10 min): 234°C Melt crystallization enthalpy: ⁇ Hmc (400°C): 49 J/g Residual melt crystallization enthalpy: ⁇ Hmc (400°C/10 min): 38 J/g Incidentally, the weight ratio of the sum of PATE recurring units to the sum of PTK recurring units was 1.0.
  • the reaction conditions upon synthesis of the copolymer were as follows:
  • Copolymer C9 The physical properties of Copolymer C9 were as follows: Melt viscosity: 100 poises (10 Pa.s) Transition temperature: Tg: 106°C (as to quench-pressed sheet) Tm: 301°C (as to polymer as polymerized) Tm: 296°C (as to quench-pressed sheet) Melt crystallization temperature: Tmc (400°C): 269°C Tmc (400°C/10 min): 220°C Melt crystallization enthalpy: ⁇ Hmc (400°C): 55 J/g Residual melt crystallization enthalpy: ⁇ Hmc (400°C/10 min): 43 J/g Incidentally, the weight ratio of the sum of PATE recurring units to the sum of PTK recurring units was 1.2.

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Claims (17)

  1. Copolymère de poly(arylène thioéther-cétone) comprenant (A) au moins un segment de poly(arylène thioéther-cétone) ayant des motifs répétés principaux de formule
    Figure imgb0050
     où -CO- et -S- sont en position para l'un par rapport à l'autre et (B) au moins un segment de poly(arylène thioéther) ayant des motifs répétés principaux de formule
    Figure imgb0051
     et ayant les propriétés (a) à (c) suivantes :
    (a) le rapport de la quantité totale du segment de poly(arylène thioéther) (B) à la quantité totale du segment de poly(arylène thiéther-cétone) (A) se situe dans la gamme de 0,05 à 5 en poids,
    (b) la moyenne en nombre du degré de polymérisation du segment de poly(arylène thioéther) (B) est supérieure à 1 mais inférieure à 10 et
    (c) ledit copolymère a une viscosité à l'état fondu de 2 à 100 000 poises (0,2 à 10⁴ Pa.s) mesurée à 350°C avec un taux de cisaillement de 1 200/s.
  2. Copolymère selon la revendication 1, dans lequel le copolymère de poly(arylène thioéther-cétone) a une température de cristallisation à l'état fondu, Tmc (400°C/10 min), d'au moins 170°C et une enthalpie de cristallisation résiduelle à l'état fondu, ΔHmc (400°C/10 min), d'au moins 10 J/g, où Tmc (400°C/10 min) et ΔHmc (400°C/10 min) sont déterminées avec un calorimètre différentiel à balayage avec une vitesse de refroidissement de 10°C/min après que le copolymère ait été maintenu à 50°C pendant 5 minutes dans une atmosphère de gaz inerte, chauffé à 400°C à la vitesse de 75°C/min, puis maintenu pendant 10 minutes à 400°C.
  3. Copolymère selon la revendication 1 ou 2, dans lequel le segment (B) a des motifs répétés principaux de formule
    Figure imgb0052
  4. Copolymère selon l'une quelconque des revendications précédentes, dans lequel le rapport de la quantité totale du segment (B) à la quantité totale du segment (A) se situe dans une gamme d'au moins 0,05 à moins de 1 en poids.
  5. Copolymère selon l'une quelconque des revendications 1 à 3, dans lequel le rapport de la quantité totale du segment (B) à la quantité totale du segment (A) se situe dans une gamme de 1 à 5 en poids.
  6. Procédé pour la production d'un copolymère de poly(arylène thioéther-cétone) comprenant (A) au moins un segment de poly(arylène thioéther-cétone) et (B) au moins un segment de poly(arylène thioéther) qui comprend au moins les deux étapes suivantes :
    i) chauffage en présence d'eau d'un amide organique solvant contenant un composé aromatique dihalogéné, qui est constitué principalement d'un dihalogénobenzène, et d'un sulfure de métal alcalin, pour synthétiser un poly(arylène thioéther) oligomère ayant des motifs répétés principaux de formule
    Figure imgb0053
     et au moins un groupe thiolate terminal, et
    ii) mélange de l'oligomère qui a été obtenu dans l'étape i) avec un composé aromatique dihalogéné constitué principalement d'au moins une dihalogénohenzophénone, choisie parmi la 4,4'-dichlorobenzophénone et la 4,4'-dibromobenzophénone, et facultativement un sulfure de métal alcalin, un amide organique solvant et/ou de l'eau, et chauffage du mélange obtenu pour former un segment de poly(arylène thioéther-cétone) ayant des motifs répétés principaux de formule
    Figure imgb0054
     dans laquelle -CO- et -S- sont en position para l'un par rapport à l'autre, pour former ainsi le copolymère ;
       lesdites première et seconde étapes i) et ii) étant effectuées dans les conditions (a) à (f) suivantes :
    (a) dans la première étape i), le rapport de la teneur en eau à la quantité d'amide organique solvant chargée est de 0,1-15 (kg/mol), le rapport de la quantité du composé aromatique dihalogéné chargée à la quantité du sulfure de métal alcalin chargée est de 0,3-0,9 (mol/mol), et la polymérisation est effectuée de telle sorte que le poly(arylène thioéther) oligomère obtenu ait au moins un groupe thiolate terminal et que la moyenne en nombre de son degré de polymérisation soit supérieure à 1 mais inférieure à 10,
    (b) dans la seconde étape ii), le rapport de la teneur en eau à la quantité d'amide organique solvant chargée est ajusté dans une gamme de 0,1-15 (mol/kg),
    (c) dans la seconde étape ii), le rapport de la quantité totale du composé aromatique dihalogéné chargée, ladite quantité totale étant la quantité du total des composés aromatiques dihalogénés comprenant le dihalogénobenzène et la dihalogénobenzophénone, à la quantité totale du sulfure de métal alcalin chargée, cette dernière quantité totale étant la quantité totale du sulfure de métal alcalin chargée dans la première étape i) et celle éventuellement chargée dans la seconde étape ii), est ajusté dans une gamme de 0,95-1,2 (mol/mol),
    (d) le rapport de la quantité chargée du composé aromatique dihalogéné constitué principalement du dihalogénobenzène dans l'étape i) à la quantité chargée du composé aromatique dihalogéné constitué principalement de la dihalogénobenzophénone dans l'étape ii) est ajusté dans une gamme de 0,1-10 (mol/mol),
    (e) la réaction de la seconde étape ii) est effectuée dans une gamme des températures de 150 à 300°C, sous réserve que le temps de réaction à 210°C et plus ne dépasse pas 10 heures, et
    (f) dans la seconde étape ii) la réaction est effectuée jusqu'à ce que la viscosité à l'état fondu du copolymère obtenu soit de 2 à 100 000 poises (0,2 à 10⁴ Pa.s) mesurée à 350°C avec un taux de cisaillement de 1 200/s.
  7. Procédé selon la revendication 6, dans lequel le poly(arylène thioéther) oligomère a des motifs répétés principaux de formule
    Figure imgb0055
  8. Procédé selon la revendication 6 ou 7, dans lequel, dans chacune des étapes i) et ii), la réaction est effectuée dans un réacteur dont au moins une portion, ladite portion étant mise en contact avec le mélange réactionnel, est faite d'un matériau résistant à la corrosion.
  9. Procédé selon la revendication 8, dans lequel le matériau résistant à la corrosion est un matériau en titane.
  10. Procédé selon l'une quelconque des revendications 6 à 9, dans lequel l'amide organique solvant est au moins une pyrrolidone choisie parmi la N-méthylpyrrolidone et la N-éthylpyrrolidone.
  11. Procédé selon l'une quelconque des revendications 6 à 10, dans lequel, lors de l'obtention du copolymère de poly(arylène thioéther-cétone), au moins 50 % en poids du copolymère obtenu sont sous forme de granules pouvant être récupérés sur un tamis ayant des ouvertures de 75 »m.
  12. Procédé pour la production d'un copolymère de poly(arylène thioéther-cétone) comprenant (A) au moins un segment de poly(arylène thioéther-cétone) et (B) au moins un segment de poly(arylène thioéther), qui comprend au moins les trois étapes suivantes :
    i) chauffage en présence d'eau d'un amide organique solvant contenant un composé aromatique dihalogéné qui est constitué principalement d'un dihalogénobenzène, et d'un sulfure de métal alcalin pour synthétiser un poly(arylène thioéther) oligomère ayant des motifs répétés principaux de formule
    Figure imgb0056
     et au moins un groupe thiolate terminal,
    ii) chauffage en présence d'eau d'un amide organique solvant contenant un composé aromatique dihalogéné qui est constitué principalement d'au moins une dihalogénobenzophénone, choisie parmi la 4,4'-dichlorobenzophénone et la 4,4'-dibromobenzophénone, et d'un sulfure de métal alcalin, pour synthétiser une poly(arylène thioéther-cétone) oligomère ayant des motifs répétés principaux de formule
    Figure imgb0057
     où -CO- et -S- sont en position para l'un par rapport à l'autre, et des atomes d'halogène terminaux, et
    iii) mélange et réaction du poly(arylène thioéther) oligomère, qui a été obtenu dans l'étape i), avec la poly(arylène thioéther-cétone) oligomère obtenue dans l'étape ii) et éventuellement de l'eau ;
       lesdites étapes un à trois i) à iii) étant effectuées dans les conditions (a) à (g) suivantes :
    (a) dans la première étape i), le rapport de la teneur en eau à la quantité d'amide organique solvant chargée est de 0,1-15 (kg/mol), le rapport de la quantité du composé aromatique dihalogéné chargée à la quantité du sulfure de métal alcalin chargée est de 0,3-0,9 (mol/mol) et la polymérisation est effectuée de telle sorte que la moyenne en nombre du degré de polymérisation du poly(arylène thioéther) oligomère soit supérieure à 1 mais inférieure à 10,
    (b) dans la seconde étape ii), le rapport de la teneur en eau à la quantité d'amide organique solvant chargée est ajusté dans une gamme de 0,1-15 (mol/kg) et la réaction est effectuée dans une gamme des températures de 60 à 300°C, sous réserve que la durée de la réaction à 210°C et plus ne dépasse pas 10 heures,
    (c) dans la troisième étape iii), le rapport de la teneur en eau à la quantité de l'amide organique solvant chargée est de 0,1-15 (mol/kg)
    (d) dans la troisième étape iii), le rapport de la quantité totale du composé aromatique dihalogéné chargée, ladite quantité totale étant la quantité du total des composés aromatiques dihalogénés comprenant le dihalogénobenzène et la dihalogénobenzophénone, à la quantité totale du sulfure de métal alcalin chargée, cette dernière quantité totale étant la quantité totale du sulfure de métal alcalin chargée dans la première étape i) et celle éventuellement chargée dans la seconde étape ii), est ajusté dans une gamme de 0,95-1,2 (mol/mol),
    (e) le rapport de la quantité chargée du composé aromatique dihalogéné constitué principalement du dihalogénobenzène dans l'étape i) à la quantité chargée du composé aromatique dihalogéné constitué principalement de la dihalogénobenzophénone dans l'étape ii) est ajusté dans une gamme de 0,1-10 (mol/mol),
    (f) la réaction de la troisième étape iii) est effectuée dans une gamme des températures de 150 à 300°C, sous réserve que le temps de réaction à 210°C et plus ne dépasse pas 10 heures, et
    (g) dans la troisième étape iii) la réaction est effectuée jusqu'à ce que la viscosité à l'état fondu du copolymère obtenu soit de 2 à 100 000 poises (0,2 à 10⁴ Pa.s) mesurée à 350°C avec un taux de cisaillement de 1 200/s.
  13. Procédé selon la revendication 12, dans lequel le poly(arylène thioéther) oligomère a des motifs répétés principaux de formule
    Figure imgb0058
  14. Procédé selon la revendication 12 ou 13, dans lequel, dans chacune des étapes i) à iii), la réaction est effectuée dans un réacteur dont au moins une portion, ladite portion étant mise en contact avec le mélange réactionnel, est faite d'un matériau résistant à la corrosion.
  15. Procédé selon la revendication 14, dans lequel le matériau résistant à la corrosion est un matériau en titane.
  16. Procédé selon l'une quelconque des revendications 12 à 15, dans lequel l'amide organique solvant est au moins une pyrrolidone choisie parmi la N-méthylpyrrolidone et la N-éthylpyrrolidone.
  17. Procédé selon l'une quelconque des revendications 12 à 16, dans lequel, lors de l'obtention du copolymère de poly(arylène thioéther-cétone), au moins 50 % en poids du copolymère obtenu sont sous forme de granules pouvant être récupérés sur un tamis ayant des ouvertures de 75 »m.
EP91303614A 1990-04-25 1991-04-23 Copolymère de polyarylène-thioéthercétone et son procédé de préparation Expired - Lifetime EP0459619B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP109481/90 1990-04-25
JP10948190 1990-04-25
JP3067554A JPH04213328A (ja) 1990-04-25 1991-03-08 ポリアリーレンチオエーテルケトン系コポリマーおよびその製造方法
JP67554/91 1991-03-08

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EP0459619A3 EP0459619A3 (en) 1992-03-11
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US5312894A (en) * 1992-04-30 1994-05-17 Kureha Kagaku Kogyo K.K. Granular high-melt-stable poly(arylene thioether-ketone) and production process thereof
JP3245253B2 (ja) * 1992-09-17 2002-01-07 呉羽化学工業株式会社 ポリアリーレンスルフィド樹脂組成物
CA2111542A1 (fr) * 1992-12-24 1994-06-25 Yoshikatsu Satake Composition du type resine de poly (sulfure d'arylene)

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH464538A (de) * 1966-03-28 1968-10-31 Inventa Ag Verfahren zur Herstellung von hitzebeständigen, linearen, thermoplastischen Polythioäthern
US3919177A (en) * 1973-11-19 1975-11-11 Phillips Petroleum Co P-phenylene sulfide polymers
JPS5925699B2 (ja) * 1980-07-16 1984-06-20 日産自動車株式会社 車両用収納ボツクス
JPS5790018A (en) * 1980-11-27 1982-06-04 Toray Ind Inc Stabilized polyphenylene sulfide and its production
JPS595100A (ja) * 1982-06-30 1984-01-11 富田　重助 遠消点定規および作図板
JPS6058435A (ja) * 1983-09-09 1985-04-04 Toray Ind Inc ポリスルフイドケトン成形物
JPS60104126A (ja) * 1983-11-10 1985-06-08 Mitsubishi Chem Ind Ltd 芳香族ポリチオエーテルケトンの製法
JPS60120720A (ja) * 1983-12-05 1985-06-28 Mitsubishi Chem Ind Ltd 芳香族ポリチオエ−テルケトンおよびその製造法
JPS6120017A (ja) * 1984-07-09 1986-01-28 Hitachi Ltd 液晶表示装置
JPS61197634A (ja) * 1985-02-28 1986-09-01 Asahi Chem Ind Co Ltd ポリ−（チオエ−テル芳香族ケトン）及びその製造方法
JPS61200127A (ja) * 1985-03-01 1986-09-04 Asahi Chem Ind Co Ltd 結晶性ポリ−（チオエ−テル芳香族ケトン）及びその製造方法
JPS6227434A (ja) * 1985-07-25 1987-02-05 ヒユ−ルス・アクチエンゲゼルシヤフト ケト基含有の単一−および共重合体ポリアリ−レンスルフイド並びにその製造方法
JPS64124A (en) * 1987-03-16 1989-01-05 Phillips Petroleum Co Improvement of melting stability of polymer
US5153264A (en) * 1988-10-25 1992-10-06 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
CA2001097C (fr) * 1988-10-25 1996-01-30 Yoshikatsu Satake Fibres a base de copolymere avec sequence de poly(sulfure d'arylene); leur preparation
US5120808A (en) * 1988-10-25 1992-06-09 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
US4962143A (en) * 1988-10-25 1990-10-09 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer fibers and production process thereof
US5153279A (en) * 1988-10-25 1992-10-06 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
US4975479A (en) * 1988-10-25 1990-12-04 Kureha Kagaku Kogyo K.K. Heat-resistant thermoplastic resin composition

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CA2040975A1 (fr) 1991-10-26
CA2040975C (fr) 1996-04-16
EP0459619A2 (fr) 1991-12-04
EP0459619A3 (en) 1992-03-11
US5391646A (en) 1995-02-21
JPH04213328A (ja) 1992-08-04
DE69110764D1 (de) 1995-08-03
KR940008991B1 (ko) 1994-09-28
US5288815A (en) 1994-02-22
KR910018442A (ko) 1991-11-30
US5391645A (en) 1995-02-21
DE69110764T2 (de) 1995-11-30

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